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WO2005090366A1 - Liquid textile-pretreating agent - Google Patents

Liquid textile-pretreating agent Download PDF

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Publication number
WO2005090366A1
WO2005090366A1 PCT/IB2005/000569 IB2005000569W WO2005090366A1 WO 2005090366 A1 WO2005090366 A1 WO 2005090366A1 IB 2005000569 W IB2005000569 W IB 2005000569W WO 2005090366 A1 WO2005090366 A1 WO 2005090366A1
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WIPO (PCT)
Prior art keywords
formula
compounds
weight
compound
composition
Prior art date
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Ceased
Application number
PCT/IB2005/000569
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French (fr)
Inventor
Manfred Jungen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Clariant International Ltd
Clariant Finance BVI Ltd
Original Assignee
Clariant International Ltd
Clariant Finance BVI Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Clariant International Ltd, Clariant Finance BVI Ltd filed Critical Clariant International Ltd
Priority to US10/593,169 priority Critical patent/US20080254695A1/en
Priority to EP05708677A priority patent/EP1737873A1/en
Priority to BRPI0508910-7A priority patent/BRPI0508910A/en
Publication of WO2005090366A1 publication Critical patent/WO2005090366A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
    • D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
    • D06M13/295—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof containing polyglycol moieties; containing neopentyl moieties
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer

Definitions

  • the present invention concerns a liquid textile-pretreating agent useful in all continuous and batch pretreatment operations which is based on phosphoric esters of alkoxylated Guerbet alcohols and is very stable to alkali not only in the formulation but also in the liquor.
  • the pretreatment of the natural or synthetic fibre materials constitutes an important basis for the further processing.
  • the various operations such as desizing, scouring, bleaching or mercerizing employ a wide range of textile chemicals, examples being surfactants, dispersants, emulsif ⁇ ers, bleaches, foam suppressants or defoamers.
  • these auxiliaries as they are known have to meet is high stability to alkali, especially in the alkaline scouring of woven cotton fabric. There is accordingly a constant need for new active compounds having a suitable performance profile.
  • n is from 1 to 3
  • x is from 4 to 12
  • R is a radical of the formula (II)
  • the present compounds are highly stable surfactants which can be present as a highly concentrated, for example 60% solution in water without any need for additives. This combines with good wettability and low foam-forming tendency into a unique performance profile. Especially the extremely high stability to alkali not only in the formulation but also in the liquor predestines these compounds for the alkaline scour, but use as a dispersant, as an emulsif ⁇ er or as a defoamer component is also possible.
  • n is 2 or 3
  • s is from 0 to 4
  • the sum total of (r + s) is from 5 to 7.
  • the index m is an average value, and a particularly preferred value for m is from 1.2 to 1.3.
  • the present compounds are prepared by alkoxylation of appropriate Guerbet alcohols as described in WO 03/091192 Al and subsequent phosphation, preferably with phosphorus pentoxide.
  • the alkylene oxide units of the Guerbet alcohols used are mostly ethylene oxide or propylene oxide units, but mainly ethylene oxide units combined with low fractions of propylene oxide or else only ethylene oxide units.
  • Phosphation is effected by portionwise addition of the phosphating agent at 90 to 120°C during 4 to 24 hours in the absence of air.
  • the present compounds can be used as such or in the form of an aqueous composition for pretreating textiles.
  • the present invention thus further provides a composition comprising an aqueous solution of one or more compounds of the formula (I) and also further auxiliaries.
  • the aqueous composition comprises 40% to 70% by weight of compound (I), although about 2% to 4% by weight can also be present in the form of the sodium salts.
  • the composition may further comprise 0.1% to 3.5% by weight of further auxiliary materials, examples being surfactants, biocides, defoamers or foam suppressants.
  • composition according to the invention is obtainable by simply mixing its constituents.
  • a preferred use of compounds of the formula (I) or of the abovementioned aqueous composition is the pretreatment of textiles in continuous or batch operations under alkaline conditions.
  • Alkali stability What is tested is the alkali stability of 5 g/1 of surfactant, with 100 ml of liquor being made up in each case. The test takes place at room temperature 20 to 25°C. The required amount of aqueous sodium hydroxide solution is weighed into a glass beaker and made up to 95 ml with demineralized water. 5 ml of a 10% surfactant solution are added to the alkali batches with stirring. The glass beakers are left to stand at room temperature for 24 hours without stirring.
  • a 1000 ml graduated cylinder 60 mm in internal diameter and 430 mm in internal height is used.
  • the test liquid is allowed to pour out from a 2 1 separating funnel through a capillary 70 mm in length and 2 mm in internal diameter from a height of 600 mm, measured from the outlet of the capillary above the floor of the cylinder.
  • 500 ml of the solution to be tested are filled into the separating funnel and allowed to flow out into the graduated cylinder through the capillary-controlled efflux rate of about 0.17 1/min.
  • a stopwatch is started and the entire volume (foam volume plus solution volume) is read off the cylinder scale. The reading is repeated after one minute.
  • the alkaline foam performance is tested using a surfactant concentration of 2 g/1 in 2° Be NaOH solution in demineralized water, with 2° Be NaOH being equivalent to 12 g/1 of NaOH solid or 30 ml/1 of NaOH 36° Be.
  • the test temperature is 20 to 25°C.
  • This test method determines the number of seconds a fabric sample takes to sink to the bottom of a glass beaker 1 1 in content, 14 cm in height and 10 cm in diameter in a surfactant solution.
  • the fabric sample used is a cotton test cloth, from EMPA Testmaterialien AG of St. Gallen, Switzerland. Circularly round discs 3.5 cm in diameter are die cut out of this cloth and dipped with a special holder into the surfactant solution. The wetting action is tested in 2° Be NaOH at

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Biochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Detergent Compositions (AREA)

Abstract

The present invention concerns a liquid textile-pretreating agent useful in all continuous and batch pretreatment operations which is based on phosphoric esters of alkoxylated Guerbet alcohols and is very stable to alkali not only in the formulation but also in the liquor. It is usually used in the form of an aqueous composition having an active content in the range from 40% to 70% by weight, with or without 0.1% to 3.5% by weight of further auxiliary materials, examples being surfactants, biocides, defoamers or foam suppressants.

Description

LIQUID TEXTILE-PRETREATING AGENT
The present invention concerns a liquid textile-pretreating agent useful in all continuous and batch pretreatment operations which is based on phosphoric esters of alkoxylated Guerbet alcohols and is very stable to alkali not only in the formulation but also in the liquor.
In grey cloth conversion, the pretreatment of the natural or synthetic fibre materials constitutes an important basis for the further processing. The various operations such as desizing, scouring, bleaching or mercerizing employ a wide range of textile chemicals, examples being surfactants, dispersants, emulsifϊers, bleaches, foam suppressants or defoamers. Among the requirements which these auxiliaries as they are known have to meet is high stability to alkali, especially in the alkaline scouring of woven cotton fabric. There is accordingly a constant need for new active compounds having a suitable performance profile.
It has now been found that, surprisingly, phosphoric esters of specific alkoxylated Guerbet alcohols are very useful for continuous and batch pretreatment of textile material. Alkoxylated Guerbet alcohols as such are known for example from WO 03/091192 Al. Although the use in formulations for the textile industry is disclosed there, no pointer is given to the excellent and surprising properties of the phosphoric esters.
The invention accordingly provides compounds of the formula (I)
Figure imgf000002_0001
where m is from 1 to 3,
Figure imgf000002_0002
x is from 4 to 12, and
R is a radical of the formula (II)
Figure imgf000003_0001
where
Figure imgf000003_0002
s is from 0 to 8, the sum total of (r + s) is from 4 to 8, and the alkyl chains may in turn be linear or branched.
The present compounds are highly stable surfactants which can be present as a highly concentrated, for example 60% solution in water without any need for additives. This combines with good wettability and low foam-forming tendency into a unique performance profile. Especially the extremely high stability to alkali not only in the formulation but also in the liquor predestines these compounds for the alkaline scour, but use as a dispersant, as an emulsifϊer or as a defoamer component is also possible.
Also of very high suitability are compounds wherein m is from 1 to 3, n is 2 or 3,
Figure imgf000003_0003
s is from 0 to 4, and the sum total of (r + s) is from 5 to 7.
Especially good properties are exhibited by compounds wherein
Figure imgf000003_0004
x is 7, r is 4, s is 2, and the sum total of (r + s) is 6.
The index m is an average value, and a particularly preferred value for m is from 1.2 to 1.3.
The present compounds are prepared by alkoxylation of appropriate Guerbet alcohols as described in WO 03/091192 Al and subsequent phosphation, preferably with phosphorus pentoxide. The alkylene oxide units of the Guerbet alcohols used are mostly ethylene oxide or propylene oxide units, but mainly ethylene oxide units combined with low fractions of propylene oxide or else only ethylene oxide units.
Phosphation is effected by portionwise addition of the phosphating agent at 90 to 120°C during 4 to 24 hours in the absence of air.
The present compounds can be used as such or in the form of an aqueous composition for pretreating textiles.
The present invention thus further provides a composition comprising an aqueous solution of one or more compounds of the formula (I) and also further auxiliaries.
Preferably, the aqueous composition comprises 40% to 70% by weight of compound (I), although about 2% to 4% by weight can also be present in the form of the sodium salts. The composition may further comprise 0.1% to 3.5% by weight of further auxiliary materials, examples being surfactants, biocides, defoamers or foam suppressants.
The composition according to the invention is obtainable by simply mixing its constituents. A preferred use of compounds of the formula (I) or of the abovementioned aqueous composition is the pretreatment of textiles in continuous or batch operations under alkaline conditions.
The examples which follow illustrate the invention.
EXAMPLES
There now follows a description of the alkoxylated Guerbet alcohols used, of the products obtained therefrom by phosphation, the aqueous formulations produced therefrom and the resulting applicatory results in table form.
The following test methods were employed:
• Alkali stability What is tested is the alkali stability of 5 g/1 of surfactant, with 100 ml of liquor being made up in each case. The test takes place at room temperature 20 to 25°C. The required amount of aqueous sodium hydroxide solution is weighed into a glass beaker and made up to 95 ml with demineralized water. 5 ml of a 10% surfactant solution are added to the alkali batches with stirring. The glass beakers are left to stand at room temperature for 24 hours without stirring.
The solutions are tested for their stability after 24 hours. Creaming and precipitates are to be noted in particular, cloudiness without visible deposits being permissible. What is to be ascertained is the concentration at which the surfactant is still stable. Alkali stability is reported in X of °Be- NaOH.
• Ross-Miles foam test The foam volume is measured after a certain amount of liquid has been poured from a certain height, instantly and after a one minute wait.
A 1000 ml graduated cylinder 60 mm in internal diameter and 430 mm in internal height is used. The test liquid is allowed to pour out from a 2 1 separating funnel through a capillary 70 mm in length and 2 mm in internal diameter from a height of 600 mm, measured from the outlet of the capillary above the floor of the cylinder.
500 ml of the solution to be tested are filled into the separating funnel and allowed to flow out into the graduated cylinder through the capillary-controlled efflux rate of about 0.17 1/min. As soon as the entire solution has flowed out, a stopwatch is started and the entire volume (foam volume plus solution volume) is read off the cylinder scale. The reading is repeated after one minute.
The alkaline foam performance is tested using a surfactant concentration of 2 g/1 in 2° Be NaOH solution in demineralized water, with 2° Be NaOH being equivalent to 12 g/1 of NaOH solid or 30 ml/1 of NaOH 36° Be. The test temperature is 20 to 25°C.
Alkaline wetting
This test method determines the number of seconds a fabric sample takes to sink to the bottom of a glass beaker 1 1 in content, 14 cm in height and 10 cm in diameter in a surfactant solution. The fabric sample used is a cotton test cloth, from EMPA Testmaterialien AG of St. Gallen, Switzerland. Circularly round discs 3.5 cm in diameter are die cut out of this cloth and dipped with a special holder into the surfactant solution. The wetting action is tested in 2° Be NaOH at
TABLE 1 Utilized alkoxylated Guerbet alcohols and other alcohols
Figure imgf000007_0001
EO, PO = ethylene oxide, propylene oxide; VI to V3 are comparative alcohols.
TABLE 2 Phosphation
Figure imgf000007_0002
Figure imgf000008_0001
TABLE 3 Aqueous formulations
Figure imgf000008_0002
Figure imgf000009_0001
Figure imgf000010_0001
Figure imgf000011_0001
Figure imgf000012_0001
Figure imgf000013_0001
TABLE 4 Applicatory results
Figure imgf000013_0002
Figure imgf000014_0001
* unless explicitly mentioned, all formations contain 60% active and 0% solubilizer, and the cloud point is > 80°C for all (applicatory advantage) n.b. not assessed; AS active substance
The examples show distinctly that the present invention's formulations of the novel phosphoric esters of certain Guerbet alcohols have a very good property profile, i.e. high stability to alkali, minimal foaming and good wetting.

Claims

1. Compounds of the formula (I)
Figure imgf000015_0001
where m is from 1 to 3, n is 2 or 3,
Figure imgf000015_0002
R is a radical of the formula (II)
H H3C
(CH2)r C H.
Figure imgf000015_0003
CH. (ii) where
Figure imgf000015_0004
the sum total of (r + s) is from 5 to 7, and the alkyl chains may in turn be linear or branched.
Compound according to Claim 1 wherein
Figure imgf000015_0005
n is 2, X is 7, r is 4, s is 2, and the sum total of (r + s) is 6.
3. Process for preparing compounds of the formula (I) according to Claims 1 or 2, characterized in that a Guerbet alcohol R-OH, where R has the meaning of the formula (II), is alkoxylated and subsequently phosphated.
4. Process according to Claim 3, characterized in that a Cι0-Guerbet alcohol is reacted with ethylene oxide and then with phosphorus pentoxide.
5. Composition comprising in aqueous solution one or more compounds of the formula (I) according to Claims 1 or 2 and also further auxiliaries.
6. Composition according to Claim 5 comprising 40% to 70% by weight of compound (I), with 2% to 4% by weight being present in the form of the sodium salt, and 0.1% to 3.5% by weight of surfactants, biocides, defoamers or foam suppressants.
7. Process for producing a composition according to Claims 5 or 6, characterized in that the compound or compounds of the formula (I) and the further constituents are mixed in an aqueous medium.
8. Use of compounds of the formula (I) according to Claims 1 or 2 or of compositions according to Claims 5 or 6 for pretreating textiles.
9. Use according to Claim 8, characterized in that pretreatment comprises continuous or batch pretreatment operations under alkaline conditions.
PCT/IB2005/000569 2004-03-17 2005-03-02 Liquid textile-pretreating agent Ceased WO2005090366A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US10/593,169 US20080254695A1 (en) 2004-03-17 2005-03-02 Liquid Textile-Pretreating Agent
EP05708677A EP1737873A1 (en) 2004-03-17 2005-03-02 Liquid textile-pretreating agent
BRPI0508910-7A BRPI0508910A (en) 2004-03-17 2005-03-02 liquid textile pretreatment agent

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP04006338.0 2004-03-17
EP04006338 2004-03-17

Publications (1)

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WO2005090366A1 true WO2005090366A1 (en) 2005-09-29

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US (1) US20080254695A1 (en)
EP (1) EP1737873A1 (en)
KR (1) KR20070005627A (en)
CN (1) CN1930177A (en)
BR (1) BRPI0508910A (en)
IN (1) IN2006CH03368A (en)
MX (1) MXPA06010103A (en)
WO (1) WO2005090366A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008012242A1 (en) 2006-07-24 2008-01-31 Basf Se Mixture for improved foaming in the extraction of petroleum or natural gas
WO2009015857A3 (en) * 2007-08-02 2009-08-20 Clariant Int Ltd Aqueous compositions containing alkoxylated phosphoric acid triesters
CN102869746A (en) * 2010-04-23 2013-01-09 巴斯夫欧洲公司 Method for producing mineral oil using surfactants based on a mixture of C32-guerbet-, C34-guerbet-, C36-guerbet-containing alkyl alkoxylates
US8389756B2 (en) 2007-08-02 2013-03-05 Clariant Finance (Bvi) Limited Method for producing alkoxylated phosphoric acid triesters
US8686033B2 (en) 2007-08-02 2014-04-01 Clariant Finance (Bvi) Limited Phosphoric acid esters containing phosphorus atoms bridged by diol units

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116143828A (en) * 2023-04-23 2023-05-23 四川科宏达集团有限责任公司 Synthetic method of phosphate surfactant with high diester content

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05140174A (en) * 1991-11-20 1993-06-08 Sakai Chem Ind Co Ltd Production of phosphoric triester
WO2002008164A1 (en) * 2000-07-21 2002-01-31 Basf Aktiengesellschaft Secondary c10-18 surfactant alcohols
DE20303420U1 (en) * 2003-03-03 2003-09-25 Sasol Germany GmbH, 22297 Hamburg Fischer-Tropsch and corresponding Guerbet alcohol mixtures, derivatives and compositions are useful e.g. in polymer, oil, cosmetic, pharmaceutical, detergent or functional fluid containing polymer surfactant and/or hydraulic fluid
WO2003091192A1 (en) * 2002-04-26 2003-11-06 Basf Aktiengesellschaft C10-alkanolalkoxylate mixtures and the use thereof

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US4453946A (en) * 1981-04-29 1984-06-12 Ciba-Geigy Corporation Dyeing assistant and use thereof in dyeing synthetic fibre material

Patent Citations (4)

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Publication number Priority date Publication date Assignee Title
JPH05140174A (en) * 1991-11-20 1993-06-08 Sakai Chem Ind Co Ltd Production of phosphoric triester
WO2002008164A1 (en) * 2000-07-21 2002-01-31 Basf Aktiengesellschaft Secondary c10-18 surfactant alcohols
WO2003091192A1 (en) * 2002-04-26 2003-11-06 Basf Aktiengesellschaft C10-alkanolalkoxylate mixtures and the use thereof
DE20303420U1 (en) * 2003-03-03 2003-09-25 Sasol Germany GmbH, 22297 Hamburg Fischer-Tropsch and corresponding Guerbet alcohol mixtures, derivatives and compositions are useful e.g. in polymer, oil, cosmetic, pharmaceutical, detergent or functional fluid containing polymer surfactant and/or hydraulic fluid

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CARIES RESEARCH , 25(1), 51-7 CODEN: CAREBK; ISSN: 0008-6568, 1991, XP009034124 *
DATABASE CHEMABS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 1994, WACHI, TOSHIO ET AL: "Preparation of phosphate triesters", XP002289140, retrieved from STN Database accession no. 1994:54693 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008012242A1 (en) 2006-07-24 2008-01-31 Basf Se Mixture for improved foaming in the extraction of petroleum or natural gas
US7842650B2 (en) 2006-07-24 2010-11-30 Basf Aktiengesellschaft Mixture for improved foaming in the extraction of petroleum or natural gas
EA018168B1 (en) * 2006-07-24 2013-06-28 Басф Се Composition for producing foams from liquids, process for extracting mineral oil and/or natural gas, process for tertiary mineral oil production process and process for drilling technique that employs foamed drilling fluid
WO2009015857A3 (en) * 2007-08-02 2009-08-20 Clariant Int Ltd Aqueous compositions containing alkoxylated phosphoric acid triesters
US8389756B2 (en) 2007-08-02 2013-03-05 Clariant Finance (Bvi) Limited Method for producing alkoxylated phosphoric acid triesters
US8686033B2 (en) 2007-08-02 2014-04-01 Clariant Finance (Bvi) Limited Phosphoric acid esters containing phosphorus atoms bridged by diol units
US8841475B2 (en) 2007-08-02 2014-09-23 Clariant Finance (Bvi) Limited Method for producing alkoxylated phosphoric acid triesters
CN102869746A (en) * 2010-04-23 2013-01-09 巴斯夫欧洲公司 Method for producing mineral oil using surfactants based on a mixture of C32-guerbet-, C34-guerbet-, C36-guerbet-containing alkyl alkoxylates

Also Published As

Publication number Publication date
BRPI0508910A (en) 2007-08-14
MXPA06010103A (en) 2006-11-01
CN1930177A (en) 2007-03-14
EP1737873A1 (en) 2007-01-03
US20080254695A1 (en) 2008-10-16
KR20070005627A (en) 2007-01-10
IN2006CH03368A (en) 2007-06-22

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